Arterial Vascular Engineering, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K984627 | AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER | DQO | 1999-07-27 | View |
| 510(k) | K983927 | GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT | DQT | 1999-03-11 | View |
| 510(k) | K971295 | AVE BRIDGE STENT SYSTEM | FGE | 1997-11-05 | View |
No matching devices.
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